Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13

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Bibliographic Details
Published in:Journal of medical genetics 2002, Vol.39 (11), p.852-856
Main Authors: Debeer, P, Bacchelli, C, Scambler, P J, De Smet, L, Fryns, J-P, Goodman, F R
Format: Report
Language:English
Online Access:Get full text
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ISSN:1468-6244